Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
  • Y10S525/902—Core-shell

Definitions

• This invention relates to a thermoplastic resin composition having excellent impact resistance, weather resistance and moldability, as well as to a process for preparing the same.
• ABS resin which forms a two-phase resin composed of resin and rubber.
• ABS resin is subject to deterioration by ultraviolet light or the like and hence exhibits poor weather resistance, because the butadiene-based polymer consituting its rubber component for imparting impact resistance to the resin has a large number of chemically unstable double bonds in its backbone.
• thermoplastic resins proposed in the prior arts the balance between the gloss and impact resistance of molded articles obtained by molding at high temperatures is not quite satisfactory. Specifically, such thermoplastic resins have the disadvantage that, when they are molded in a wide temperature range extending from low to high temperatures, the resulting molded articles cannot always retain a high gloss. Thus, a thermoplastic resin having a combination of excellent impact resistance, weather resistance and moldability has not been available in the prior arts.
• thermoplastic resin composition having a combination of excellent impact resistance, weather resistance and moldability can be obtained, by forming a graft copolymer resin through polymerization of at least one monomer selected from the group consisting of aromatic vinyl compounds and ethylenically unsaturated compounds, in the presence of a latex containing a composite-structured acrylic rubber whose particles are composed of a core consisting of an enlarged diene rubber prepared by treating a diene rubber latex of smaller particle size with an acid group-containing copolymer latex, and an outer layer consisting of a crosslinked acrylate polymer derived from an acrylic ester as the main component and formed by the combined use of a graft-linking agent and a cross-linking agent.
• the present invention has been completed
• thermoplastic resin composition having excellent impact resistance, weather resistance and moldability which comprises (A) a graft copolymer resin (3) obtained by polymerizing 10 to 95 parts by weight of at least one monomer (2) selected from the group consisting of aromatic vinyl compounds and ethylenically unsaturated compounds of the general formula where R is -H or -CH 3 , X is -CN or -COOR 1 , and R is an alkyl group having 1 to 8 carbon atoms, in the presence of 90 to 5 parts by weight (on a solid basis) of a latex of a composite-structured crosslinked acrylic rubber (1) whose particles are composed of 2 to 80% by weight of a core consisting of a diene rubber (i) enlarged by treatment with an acid group-containing copolymer latex, and 20 to 98% by weight of an outer layer consisting of a crosslinked acrylate polymer (ii) derived from an acrylic ester as the main component and formed by the combined use of a
• thermoplastic resin composition having excellent impact resistance, weather resistance and moldability which comprises (A) forming a graft copolymer resin (3) by polymerizing 10 to 95 parts by weight of at least one monomer (2) selected from the group consisting of aromatic vinyl compounds and ethylenically unsaturated compounds of the general formula where R is -H or -CH3, X is -CN or -COOR 1 , and R 1 is an alkyl group having 1 to 8 carbon atoms, in the presence of 90 to 5 parts by weight (on a solid basis) of a latex of a composite-structured crosslinked acrylic rubber (1) whose particles are composed of 2 to 80% by weight of a core consisting of a diene rubber (i) enlarged'by treatment with an acid group-containing copolymer latex, and 20 to 98% by weight of an outer layer consisting of a crosslinked acrylate polymer (ii) derived from an acrylic ester as the main component
• the enlarged diene rubber (i) is 1,3-polybutadiene homopolymer or a copolymer comprising 50% by weight or more of 1,3-butadiene units.
• copolymers examples include butadiene-aromatic vinyl compound copolymers such as butadiene-styrene copolymer and butadiene-vinyltoluene copolymer; butadiene-acrylonitrile copolymer; butadiene- methacrylonitrile copolymer; butadiene-alkyl acrylate copolymers such as butadiene-methyl acrylate copolymer, butadiene-ethyl acrylate copolymer, butadiene-butyl acrylate copolymer and butadiene-2-ethylhexyl acrylate copolymer; butadiene-alkyl methacrylate copolymers such as butadiene-methyl methacrylate copolymer and butadiene-ethyl methacrylate copolymer; and the like, and further include terpolymers comprising 50% by weight or more of 1,3-butadiene units.
• an acid group-containing copolymer latex is used to enlarge the particles present in a latex of the aforesaid diene rubber. It is essential that this acid group-containing copolymer latex be composed of an acid group-containing monomer and an alkyl acrylate.
• Useful examples of the acid group-containing monomer include acrylic acid, methacrylic acid, itaconic acid and crotonic acid.
• the alkyl acrylate there is used at least one alkyl acrylate of 1 to 12 carbon atoms in the alkyl group.
• the acid group-containing monomer is used in an amount of 3 to 30% by weight based on the total amount of the monomers constituting the acid group-containing copolymer. If the amount of acid group-containing monomer used is less than 3% by weight, little particle-enlarging effect will be produced. If it is greater than 30% by weight, the particle-enlarging effect is so powerful that there may be an undesirable tendency toward the formation of excessively large particles having a diameter of greater than 1 ⁇ m.
• the optimum content of the acid group-containing monomer also depends on the degree of hydrophilic property of the alkyl acrylate used. Where the alkyl acrylate has a high degree of hydrophilic property, a particle-enlarging effect is produced at a low content of the acid group-containing monomer. In this case, a high content of the acid group-containing monomer is undesirable because the latex may be destroyed. On the contrary, where the alkyl acrylate has a low degree of hydrophilic property, little particle-enlarging effect is produced at a low content of the acid group-containing monomer. In other words, a satisfactory effect cannot be produced unless the content of the acid group-containing monomer exceeds a certain level.
• the optimum content of the acid group-containing monomer is in the range of 5 to 10% by weight.
• hydrophobic alkyl acrylates having 4 or more carbon atoms in the alkyl group such as butyl acrylate and 2-ethylhexyl acrylate, are used, the optimum content of the acid group-containing monomer is in the range of 13 to 20% by weight.
• the acid group-containing copolymer is used in the form of a latex. Its particle size has a great influence on its particle-enlarging power, and the preferred range of its average particle diameter is from 0.05 to 0.2 pm. If its average particle diameter is smaller than 0.05 ⁇ m, its particle-enlarging power will be significantly reduced. If it is larger than 0.2 pm, the enlarged rubber particles will have an excessively large diameter and, therefore, they may become unstable and tend to agglomerate during subsequent graft polymerization.
• the particle enlargement of the diene rubber is effected by adding the acid group-containing copolymer latex to a latex of the diene rubber having a small particle diameter of, for example, 0.04 to 0.2 pm.
• the acid group-containing copolymer latex is added in an amount of 0.1 to 10 parts by weight (on a solid basis) per 100 parts by weight (on a solid basis) of the base diene rubber latex. It is especially preferable to add the acid group-containing copolymer latex in an amount of 0.5 to 5 parts by weight.
• the average particle diameter of the enlarged diene rubber (i) latex is adjusted to a value of 0.15 to 1 pm.
• the resulting latex of the composite-structured crosslinked acrylic rubber containing the aforesaid rubber as a core will have an average particle diameter of 0.18 to 3 ⁇ m which is preferable from the viewpoint of the appearance of molded articles.
• the latex of the base diene rubber in the treatment for enlarging the particles of the diene rubber in accordance with the present invention, it is preferable to maintain the latex of the base diene rubber at a pH of 7 or higher. If its pH is in the acid region, the addition of the acid group-containing copolymer latex will produce little particle-enlarging effect, so that it may be difficult to prepare the desired resin composition of the present invention advantageously.
• pH adjustment may be made either during the polymerization of the base diene rubber or prior to the particle-enlarging treatment.
• the crosslinked acrylate polymer (ii) constituting the outer layer of rubber particles is formed by the combined use of a graft-linking agent and a cross-linking agent.
• a graft-linking agent for example, alkyl acrylates of 1 to 12 carbon atoms in the alkyl group, such as methyl, ethyl, n-propyl, n-butyl, 2-ethylhexyl or n-lauryl; haloalkyl acrylates such as chloroethyl acrylate; aromatic acrylic esters such as benzyl acrylate or phenetyl acrylate; and the like.
• the monomers copolymerizable with these acrylic esters include methacrylic esters such as methyl methacrylate and butyl methacrylate; acrylonitrile; styrene; and the like. According to need, these monomers may be used in an amount of less than 50% by weight of the polymer (ii).
• the graft-linking agent used for this purpose is a compound which contains 2 or 3 unsaturated groups having addition polymerizability and in which these unsaturated groups are markedly different from each other in polymerization reactivity, and examples thereof include allyl esters of unsaturated acids such as acrylic acid, methacrylic acid, maleic acid, fumaric acid, cyanuric acid and isocyanuric acid. Among these compounds, allyl methacrylate, triallyl cyanurate and triallyl isocyanurate are preferably used. These compounds may be used either alone or in an admixture of two or more.
• the cross-linking agent is a compound which contains a plurality of unsaturated groups having addition polymerizability and in which these unsaturated groups are almost equal to or slightly different rrom each other in polymerization reactivity, and examples thereof include diacrylic or dimethacrylic esters of polyalkylene glycols and divinylbenzene.
• diacrylic or dimethacrylic esters of polyalkylene glycols and divinylbenzene examples thereof include diacrylic or dimethacrylic esters of polyalkylene glycols and divinylbenzene.
• ethylene glycol dimethacrylate, 1,3-butanediol dimethacrylate and divinylbenzene are preferably used. These compounds may be used either alone or in an admixture of two or more.
• the particles of the enlarged diene rubber (i) can be covered with the crosslinked acrylate polymer (ii) in the following manner:
• This polymerization is carried out in the presence of a radical initiator by adding the monomer (2) to the latex at a time, in portions or continuously. Where a large amount of monomer is to be added, continuous pouring is preferred in order to maintain the melt flow properties of the resulting polymer and promote the formation of a graft polymer.
• Typical examples of the aforesaid aromatic vinyl compounds include styrene, a-methylstyrene and vinyltoluene.
• the graft copolymer resin (3) thus obtained may be directly used as the thermoplastic resin composition of the present invention.
• this graft copolymer resin (3) may also be used in the form of a blend obtained by blending it with a separately prepared rigid thermoplastic resin (4) in such a proportion that the amount of the composite-structured crosslinked acrylic rubber (1) present in the resulting resin composition is 5 to 80% by weight based on the total amount of (3) and (4).
• the aforesaid rigid thermoplastic resin (4) there may be used any thermoplastic resin that is rigid at ordinary temperatures.
• aromatic vinyl compound-acrylonitrile copolymers more preferably styrene-acrylonitrile copolymer, a-methylstyrene-acrylonitrile copolymer and styrene-a-methylstyrene-acrylonitrile terpolymer; aromatic vinyl compound-methyl methacrylate copolymers, more preferably styrene-methyl methacrylate copolymer; aromatic vinyl compound-acrylonitrile-methyl methacrylate terpolymers, more preferably styrene-acrylonitrile-methyl methacrylate terpolymer; aromatic vinyl compound-acrylonitrile-lower alkyl acrylate terpolymers; acrylonitrile-lower alkyl acrylate copolymers; polymethyl methacrylate; polymers containing N-phenylmaleimide as an essential component; and polycarbonates.
• These rigid thermoplastic resins may be used either alone or in an admixture of two or
• thermoplastic resin composition prepared by the process of the present invention and having excellent impact resistance, weather resistance and moldability can additionally contain various colorants such as dyes and pigments; light or heat stabilizers; granular, powdery or fibrous inorganic fillers and organic fillers; and blowing agents, according to need.
• This composition can be processed by various processing techniques such as injection molding or extrusion molding, and can be used as a variety of molded articles having excellent impact resistance and weather resistance, or as a component of laminated structures (for example, as the outermost layer exposed to sunlight).
• Particle diameters were obtained by determining the particle diameter of a rubber or resin latex by electron microscopy, constructing a calibration curve using the absorbance at 700 nm of a diluted solution (0.15 g/t) of the latex, measuring the absorbance of the latex to be tested, and determining its particle diameter by reference to the calibration curve.
• the gel content and degree of swelling of composite-structured crosslinked acrylic rubbers (1) were calculated from the following equations: where W 0 is the original weight of a sample, W 1 is the weight of the sample which has been soaked in about 150 volumes of methyl ethyl ketone and allowed to stand at 30°C for 24 hours, and W 2 is the absolute dry weight of the same sample,
• a base rubber (a-1) was synthesized as follows:
• a mixture consisting of the above ingredients was charged into another polymerization apparatus and polymerized at 70°C for 4 hours, resulting in a degree of conversion of 98%. Thus, there was obtained a latex having an average particle diameter of 0.08 ⁇ m.
• To 100 parts (on a solid basis) of the latex of the base rubber (a-I) was added 2 parts (on a solid basis) of the above latex of the acid group-containing copolymer (B) with stirring. This mixture was further stirred for 30 minutes to obtain an enlarged diene rubber latex (A-I) having an average particle diameter of 0.27 ⁇ m.
• a base rubber (a-2) was synthesized as follows:
• a mixture consisting of the above ingredients was charged into a 100-liter autoclave and polymerized at 50°C. The polymerization was almost completed in 9 hours, resulting in a degree of conversion of 96%.
• a base rubber latex (a-2) having an average particle diameter of 0.08 ⁇ m and a pH of 8.8.
• To 100 parts (on a solid basis) of this rubber latex was added 2 parts (on a solid basis) of the aforesaid latex of the acid group-containing copolymer (B) with stirring. This mixture was stirred for 30 minutes to obtain an enlarged diene rubber latex (A-2) having an average particle diameter of 0.28 ⁇ m.
• latices of composite-structured crosslinked acrylic rubbers C-2, C-3 and C-4 were prepared under the same conditions as described above, except that the type and amount of enlarged diene rubber latex used and the types and amounts of monomers used for the formation of the crosslinked acrylate polymer were varied as shown in Table 1. The results thus obtained are shown in Table 1.
• graft copolymers D-2 to D-5 were prepared under the same conditions as described above, except that the type and amount of composite-structured crosslinked acrylic rubber latex used and the types and amounts of monomers used for graft polymerization were varied as shown in Table 2.
• Each of the latices D-1 to D-5 prepared in the above-described manner was coagulated by being added, with stirring, to 3 volumes of a 0.15% aqueous solution (at 90°C) of aluminum chloride (AlCl 3 ⁇ 6H 2 O).
• the coagulation vessel was heated to an internal temperature of 93°C and allowed to stand for 5 minutes. After cooling, the resulting coagulum was dehydrated by means of a centrifugal dehydrator, washed and then dried.
• a centrifugal dehydrator To 100 parts of each of the resulting powders of the graft copolymers D-1 to D-4 were added 1 part of barium stearate, 0.1 part of a phenolic antioxidant (commercially available from Kawaguchi Kagaku Co. under the trade name of AN TAGE W-300), and 0.5 part of an ultraviolet light absorber (commercially available from Ciba-Geigy Limited under the trade name of TINUVIN P). This mixture was blended in a Henschel mixer at 2000 rpm for 5 minutes. Then, the resulting blend was pelletized in a 40 mm ⁇ extruder having a cylinder temperature of 220°C.
• pellets E-1 to E-4 were formed of the graft copolymers D-1 to D-4, respectively.
• aMS acrylonitrile- a-methylstyrene copolymer resin
• pellets E-8 and E-9 were obtained in substantially the same manner as described in connection with the preparation of C-2, D-2 and E-2 in Example 2 and the preparation of C-4, D-4 and E-4 in Example 4, respectively.
• 0.48 parts or 0.3 parts of AMA alone i.e., with the omission of EDMA was used in the procedures for the preparation of the composite-structured crosslinked acrylic rubbers C-2 and C-4 in Examples 2 and 4, respectively.
• the resulting blend was extruded.
• the resulting blend was extruded.
• the resulting crosslinked resin latex had an average particle diameter of 0.26 ⁇ m.
• the resulting crosslinked acrylic rubber containing a core consisting of the aforesaid crosslinked resin had a degree of swelling of 8.0, a gel content of 90%, and an average particle diameter of 0.30 pm.
• the resulting latex was coagulated by adding it, with stirring, to 5 volumes of an aqueous solution of calcium chloride.
• the resulting coagulum was dehydrated by means of a centrifugal dehydrator, washed and then dried to obtain a graft polymer (D-7) having a high rubber content.
• Gloss was measured with a digital variable- angle glossmeter (manufactured by Suga Test Instruments Co.) at an angle of incidence of 60°.
• Izod impact strength was measured according to the procedure described in ASTM D-256.
• MI Melt flow index
• melt flow index was determined according to the procedure (200°C, 5 kg) described in ASTM D-1238.
• thermoplastic resin compositions of the present invention comprising a graft copolymer resin formed by using a composite-structured acrylic rubber containing a core of diene rubber
• the balance between the gloss and impact strength of molded articles over a wide temperature range extending from low to high temperatures can be improved without sacrificing their attractive appearance or excellent weather resistance, through the combined use of a graft-linking agent and a cross-linking agent for the formation of a crosslinked structure in the outer layer consisting of an acrylate polymer.

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• 1986
  • 1986-02-06 JP JP61024533A patent/JPS62181312A/ja active Granted
• 1987
  • 1987-01-30 CA CA000528660A patent/CA1270586A/en not_active Expired - Lifetime
  • 1987-02-03 EP EP87101423A patent/EP0231933B2/de not_active Expired - Lifetime
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